Canonical Allele Identifier: PA916036962
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68564
ClinVar RCV Id: RCV000059439
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Met900Arg
CA285003
NM_001353961.2:c.2699T>G